rs7582694

Variant in the STAT4 gene (Signal Transducer and Activator of Transcription 4)

rs7582694 is a single nucleotide polymorphism (SNP) in the STAT4 gene, involved in IL-12 and IFN-alpha signaling. Variants at this position have been studied in relation to immune function, metabolism, and chronic illness.

This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.

What is the rs7582694 variant?

rs7582694 is a SNP (single nucleotide polymorphism) in the STAT4 (Signal Transducer and Activator of Transcription 4) gene. It belongs to the Immune Signaling category and is part of the JAK-STAT Pathway biological cluster. STAT4 mediates IL-12 and IFN-alpha signals to drive Th1 differentiation and natural killer cell activation.

Biological role and pathway

This variant sits within the STAT4 gene, which is involved in the IL-12 and IFN-alpha signaling pathway. Genes within the JAK-STAT Pathway cluster work together to maintain balanced function across interconnected biological systems.

Variants in genes within this pathway may influence an individual's predisposition to altered function — particularly under conditions of physiological stress such as viral infection or prolonged illness.

rs7582694 and Long COVID / ME-CFS research

STAT4 variants affecting Th1/Th17 immune polarization may influence susceptibility to autoimmune features of Long COVID.

This information is based on published research and does not constitute medical advice. See references below.

Parent gene: STAT4

rs7582694 is one of 2 known variants in the STAT4 gene. To understand the full biological context of this variant, explore the parent gene page.

View STAT4 gene page →

Conditions studied in relation to rs7582694

Research into STAT4 variants including rs7582694 has explored associations with the following conditions. These are areas of scientific investigation and do not imply causation.

Genetic insights from DNA data

Consumer DNA files from 23andMe, AncestryDNA, and MyHeritage contain raw SNP data. When you upload your file to ChronicDNA, the analysis engine checks your genotype against a curated panel of 80+ genes selected for their relevance to Long COVID, ME/CFS, and connected biological pathways - some of which may include STAT4 and the rs7582694 variant.

The report is educational - it explains which variants you carry, what the research says about them, and how they fit into the biological pathways most relevant to chronic illness. Results are presented in plain English with appropriate scientific context, no medical jargon, no scare tactics. All results should be discussed with a qualified healthcare provider.

Other variants in the STAT4 gene

The following variants in STAT4 are also studied in relation to chronic illness and may be analysed together for a more complete picture.

Frequently asked questions

What is the rs7582694 variant in the STAT4 gene?

rs7582694 is a single nucleotide polymorphism (SNP) located in the STAT4 (Signal Transducer and Activator of Transcription 4) gene, which is involved in IL-12 and IFN-alpha signaling. STAT4 mediates IL-12 and IFN-alpha signals to drive Th1 differentiation and natural killer cell activation.

How may the rs7582694 variant relate to Long COVID or ME/CFS?

STAT4 variants affecting Th1/Th17 immune polarization may influence susceptibility to autoimmune features of Long COVID.

Can a consumer DNA test detect the rs7582694 variant?

Many consumer DNA tests such as 23andMe, AncestryDNA, and MyHeritage genotype common SNPs. ChronicDNA analyses your raw DNA file and reports on variants studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.

Find out if you carry the rs7582694 variant

Upload your DNA data from 23andMe, AncestryDNA, or MyHeritage and receive a personalised report covering >80 genes relevant to Long COVID and ME/CFS.

Get Your Personalised DNA Report

Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for STAT4 and its variants. This is not an exhaustive literature review.

  • [1]PMID: 29925876
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation